Single cell RNA-sequencing of Ewing sarcoma tumors demonstrates transcriptional heterogeneity and clonal evolution
肉瘤
生物
基因
小儿癌症
核糖核酸
癌症研究
原发性肿瘤
疾病
癌症
遗传学
转移
病理
医学
作者
Andrew Goodspeed,Avery Bodlak,Alexis B. Duffy,Sarah Nelson-Taylor,Naoki Oike,Timothy Porfilio,Ryota Shirai,Deandra Walker,Amy Treece,Jennifer O. Black,Nathan Donaldson,Carrye R. Cost,Tim Garrington,Brian Greffe,Sandra Luna‐Fineman,Jenna Demedis,Jessica Lake,Etienne Danis,Michael R. Verneris,Daniel L. Adams
Abstract Ewing sarcoma is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those with localized disease. Here, we utilized single cell RNA-sequencing to characterize the transcriptional landscape of primary Ewing sarcoma tumors and surrounding tumor microenvironment (TME). Copy-number analysis identified subclonal evolution within patients prior to treatment. Primary tumor samples demonstrate a heterogenous transcriptional landscape with several conserved gene expression programs, including those composed of genes related to proliferation and EWS targets. Single cell RNA-sequencing and immunofluorescence of circulating tumor cells at the time of diagnosis identified TSPAN8 as a novel therapeutic target.